نتایج جستجو برای: lyso

تعداد نتایج: 832  

2009
T. Fraser K. Stobart

T o analyse the involvement of the plastidial lysophosphatidylcholine (lyso-PC) acyltransferase in the import of the extraplastidial lipid precursors required for eukaryotic plastid lipid synthesis, we plan to obtain transgenic plants. Since no sequence of lyso-PC acyltransferase is known, the purification of this enzyme has been undertaken to establish its sequence. First we determined the con...

Journal: :Infection and immunity 1990
S Kasimir W Schönfeld J E Alouf W König

The production of delta-toxin is supposed to be responsible for various pathophysiological effects during infection with Staphylococcus aureus. We compared the effects of delta-toxin with the structurally related bee venom toxin melittin on granulocyte functions and inflammatory mediator release. Delta-toxin and melittin induced a rapid Ca2+ influx, as was shown by fluorescence detection. Furth...

Journal: :Journal of lipid research 1987
R Bittman N M Witzke T C Lee M L Blank F Snyder

Two platelet-activating factor (PAF) analogs containing a methyl group at C2 of the glycerol moiety were synthesized, and some of their biochemical properties were investigated. 1-O-Hexadecyl-2-C,O-dimethyl-rac-glycero-3-phosphocholine (2-methyl-2-methoxy PAF) was prepared in a synthetic scheme beginning with the etherification of 2-methylpropen-1-ol. A reaction sequence involving hydroxylation...

Journal: :Circulation. Cardiovascular genetics 2014
Markus Niemann Arndt Rolfs Stefan Störk Bart Bijnens Frank Breunig Meinrad Beer Georg Ertl Christoph Wanner Frank Weidemann

BACKGROUND Currently, no method is available to identify α-galactosidase A (agalA) mutations determining clinically relevant Fabry disease. In our largest European Fabry cohort, we investigated whether a biomarker, specific for the defect, could stratify persons at risk. METHODS AND RESULTS A total of 124 individuals with agalA mutations were investigated with a comprehensive clinical workup,...

2002
Lisa A. Teather Robert K.K. Lee Richard J. Wurtman

The phospholipid mediator platelet-activating factor (PAF) increased the release of prostaglandin E (PGE ) from astrocyte-enriched 2 2 cortical cell cultures in a concentrationand time-dependent manner. The nonhydrolyzable PAF analog methylcarbamyl-PAF (mc-PAF), the PAF intermediate lyso-PAF, and arachidonic acid (AA) also produced this effect. In contrast, phosphatidlycholine (PC) and lyso-PC,...

2009
Lisa M. Fox Daryl G. Cox Jennifer L. Lockridge Xiaohua Wang Xiuxu Chen Louise Scharf David L. Trott Rachel M. Ndonye Natacha Veerapen Gurdyal S. Besra Amy R. Howell Mark E. Cook Erin J. Adams William H. Hildebrand Jenny E. Gumperz

Natural killer T (NKT) cells are a subset of T lymphocytes with potent immunoregulatory properties. Recognition of self-antigens presented by CD1d molecules is an important route of NKT cell activation; however, the molecular identity of specific autoantigens that stimulate human NKT cells remains unclear. Here, we have analyzed human NKT cell recognition of CD1d cellular ligands. The most clea...

Journal: :The Biochemical journal 2003
Emyr Lloyd-Evans Dori Pelled Christian Riebeling Anthony H Futerman

Recently, we demonstrated that the GSL (glycosphingolipid), GlcCer (glucosylceramide), modulates Ca2+ release from intracellular stores and from microsomes by sensitizing the RyaR (ryanodine receptor), a major Ca2+-release channel of the endoplasmic reticulum, whereas the lyso derivative of GlcCer, namely GlcSph (glucosylsphingosine), induced Ca2+ release via a mechanism independent of the RyaR...

Journal: :Journal of lipid research 2005
Tetsuto Nakagawa Akio Morotomi Motohiro Tani Noriyuki Sueyoshi Hironobu Komori Makoto Ito

GM1a [Gal beta1-3GalNAc beta1-4(NeuAc alpha2-3)Gal beta1-4Glc beta1-1Cer] is known to support and protect neuronal functions. However, we report that alpha-linolenic acid-containing GM1a (C18:3-GM1a), which was prepared using the reverse hydrolysis reaction of sphingolipid ceramide N-deacylase, induced apoptosis in neuronal cells. Intranucleosomal DNA fragmentation, chromatin condensation, and ...

2015
YOUN-JEONG SHIN YEO JIN JEON NAMHEE JUNG JOO-WON PARK HAE-YOUNG PARK SUNG-CHUL JUNG

Fabry disease is an X-linked lysosomal storage disorder caused by mutations in the gene encoding the α-galactosidase A (α-Gal A) lysosomal enzyme, which results in globotriaosylceramide (Gb3) storage in vascular endothelial cells and different cell types throughout the body. Involvement of the kidney and heart is life threatening, and fibrosis of these organs is considered to be involved in the...

Journal: :Bioscience, Biotechnology, and Biochemistry 1995

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